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Publications

Appropriately aggregate holistic technologies via accurate expertise. Intrinsicly strategize worldwide initiatives and premium methodologies.

Comment on 'Lack of evidence for associative learning in pea plants'.

Gagliano M. et al, (2020), Elife, 9

Heritability of haemodynamics in the ascending aorta.

McGurk KA. et al, (2020), Sci Rep, 10

Is disrupted sleep a risk factor for Alzheimer’s disease? Evidence from a two-sample Mendelian randomization analysis

Anderson E. and KYLE S., (2020), International Journal of Epidemiology

Response to Comment on Satin et al. "Take Me To Your Leader": An Electrophysiological Appraisal of the Role of Hub Cells in Pancreatic Islets. Diabetes 2020;69:830-836.

Satin LS. and Rorsman P., (2020), Diabetes, 69, e12 - e13

Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease.

Nomura A. et al, (2020), Circ Genom Precis Med

Hypoxia regulates GR function through multiple mechanisms involving microRNAs 103 and 107.

Yang N. et al, (2020), Mol Cell Endocrinol, 518

Erratum: Interaction of Axonal Chondrolectin with Collagen XIXa1 Is Necessary for Precise Neuromuscular Junction Formation (Cell Reports (2019) 29(5) (1082–1098.e10), (S2211124719312215), (10.1016/j.celrep.2019.09.033))

Oprişoreanu AM. et al, (2020), Cell Reports, 32

Peripancreatic adipose tissue protects against high-fat-diet-induced hepatic steatosis and insulin resistance in mice.

Chanclón B. et al, (2020), Int J Obes (Lond)

Differential occupational risks to healthcare workers from SARS-CoV-2 observed during a prospective observational study.

Eyre DW. et al, (2020), Elife, 9

Insomnia as a mediating therapeutic target for depressive symptoms: A sub-analysis of participant data from two large randomized controlled trials of a digital sleep intervention.

Henry AL. et al, (2020), J Sleep Res

Longitudinal MEMRI analysis of brain phenotypes in a mouse model of Niemann-Pick Type C disease

Rallapalli H. et al, (2020), NeuroImage, 217

Genetic Predisposition to Coronary Artery Disease in Type 2 diabetes

van Zuydam NR. et al, (2020), Circulation: Genomic and Precision Medicine

An ALS-linked mutation in TDP-43 disrupts normal protein interactions in the motor neuron response to oxidative stress.

Feneberg E. et al, (2020), Neurobiol Dis

Reduced axonal caliber and structural changes in a rat model of Fragile X syndrome with a deletion of a K-Homology domain of Fmr1.

Golden CEM. et al, (2020), Transl Psychiatry, 10

Amyotrophic lateral sclerosis with a heterozygous D91A SOD1 variant and classical ALS-TDP neuropathology.

Feneberg E. et al, (2020), Neurology

CSF extracellular vesicle proteomics demonstrates altered protein homeostasis in amyotrophic lateral sclerosis

THOMPSON A. et al, (2020), Clinical Proteomics

The ALIOS diet in male and female rodents recapitulates the clinical and transcriptomic features of NAFLD and NASH.

Harris SE. et al, (2020), Am J Physiol Gastrointest Liver Physiol

Nanopore direct RNA sequencing detects differential expression between human cell populations

Gleeson J. et al, (2020), bioRxiv

Crossover to Photodynamic Therapy or Micropulse Laser After Failure of Primary Treatment of Chronic Central Serous Chorioretinopathy: The REPLACE Trial

van Rijssen TJ. et al, (2020), American Journal of Ophthalmology, 216, 80 - 89

Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits.

Banks GT. et al, (2020), Sci Adv, 6

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